A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16969783



Internal ID47171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:133894739..133896215hg38UCSC Ensembl
chr6:134215877..134217353hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg381477
hg191477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470770
Supporting Variants
Samples
Known GenesTCF21
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16969783
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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